Canonical Allele Identifier: CA351501629
Gene: RAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12590801A>G , CM000665.2:g.12590801A>G GRCh38
NC_000003.11:g.12632300A>G , CM000665.1:g.12632300A>G GRCh37
NC_000003.10:g.12607300A>G NCBI36
NG_007467.1:g.78379T>C , LRG_413:g.78379T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251849.9:c.1367T>C ENSP00000251849.4:p.Met456Thr
ENST00000442415.7:c.1427T>C MANE Select ENSP00000401888.2:p.Met476Thr
ENST00000251849.8:c.1367T>C ENSP00000251849.4:p.Met456Thr
ENST00000423275.5:c.*1044T>C ENSP00000401088.1:p.=
ENST00000432427.2:n.1004T>C ENSP00000398591.2:p.Met335Thr
ENST00000442415.6:c.1427T>C ENSP00000401888.2:p.Met476Thr
ENST00000460610.1:n.324T>C
ENST00000465826.5:n.724T>C
ENST00000475353.1:n.535T>C
ENST00000494557.1:n.383T>C
NM_002880.3:c.1367T>C , LRG_413t1:c.1367T>C NP_002871.1:p.Met456Thr
XM_005265355.1:c.1367T>C XP_005265412.1:p.Met456Thr
XM_005265357.1:c.1268T>C XP_005265414.1:p.Met423Thr
XM_005265358.3:c.1124T>C XP_005265415.1:p.Met375Thr
XM_005265359.3:c.1025T>C XP_005265416.1:p.Met342Thr
XM_005265360.1:c.1367T>C XP_005265417.1:p.Met456Thr
XM_011533974.1:c.1367T>C XP_011532276.1:p.Met456Thr
XM_011533975.1:c.1124T>C XP_011532277.1:p.Met375Thr
NM_001354689.1:c.1427T>C NP_001341618.1:p.Met476Thr
NM_001354690.1:c.1367T>C NP_001341619.1:p.Met456Thr
NM_001354691.1:c.1124T>C NP_001341620.1:p.Met375Thr
NM_001354692.1:c.1124T>C NP_001341621.1:p.Met375Thr
NM_001354693.1:c.1268T>C NP_001341622.1:p.Met423Thr
NM_001354694.1:c.1184T>C NP_001341623.1:p.Met395Thr
NM_001354695.1:c.1025T>C NP_001341624.1:p.Met342Thr
NR_148940.1:n.1895T>C
NR_148941.1:n.1841T>C
NR_148942.1:n.1780T>C
XM_011533974.3:c.1367T>C XP_011532276.1:p.Met456Thr
XM_017006966.1:c.1268T>C XP_016862455.1:p.Met423Thr
NM_001354689.3:c.1427T>C MANE Select NP_001341618.1:p.Met476Thr
NM_001354690.2:c.1367T>C NP_001341619.1:p.Met456Thr
NM_001354691.2:c.1124T>C NP_001341620.1:p.Met375Thr
NM_001354692.2:c.1124T>C NP_001341621.1:p.Met375Thr
NM_001354693.2:c.1268T>C NP_001341622.1:p.Met423Thr
NM_001354694.2:c.1184T>C NP_001341623.1:p.Met395Thr
NM_001354695.2:c.1025T>C NP_001341624.1:p.Met342Thr
NR_148940.2:n.1811T>C
NR_148941.2:n.1757T>C
NR_148942.2:n.1696T>C
NM_001354690.3:c.1367T>C NP_001341619.1:p.Met456Thr
NM_001354691.3:c.1124T>C NP_001341620.1:p.Met375Thr
NM_001354692.3:c.1124T>C NP_001341621.1:p.Met375Thr
NM_001354693.3:c.1268T>C NP_001341622.1:p.Met423Thr
NM_001354694.3:c.1184T>C NP_001341623.1:p.Met395Thr
NM_001354695.3:c.1025T>C NP_001341624.1:p.Met342Thr
NM_002880.4:c.1367T>C NP_002871.1:p.Met456Thr
NR_148940.3:n.1811T>C
NR_148941.3:n.1757T>C
NR_148942.3:n.1696T>C